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Quantitative data relating to dendritic parameters for each reconstructed neuron were obtained using the Neurolucida Explorer software.

Whole-cell recordings from 14 16 DIV pyramidal neurons were obtained using a partly modified method of that previously reported [34].

Nuclear extracts for control or etoposide-treated MESC2.10 neurons were obtained using the cell fractionation kit from pierce according to the instructions provided.

Whole-cell recordings from LGN relay neurons were obtained using 2- to 3-MΩ borosilicate glass electrodes filled with internal solution containing (in mM) 130 K-gluconate, 10 EGTA, 10 HEPES, 4 NaCl, 4 MgATP, 1 CaCl2, 0.5 NandTP, and 0.4 K2-Lucifer yellow.

Cases where single neuron clones were obtained using this method are labeled with red numbers.

For Δψm measurements, 25 nM TMRM was included and cells were incubated for 45 min. Z-stacks of >20 neurons per clone were obtained using a Zeiss LSM confocal microscope.

Unbiased stereological estimates of the total number of VMAT2-positive neurons per SNpc were obtained using the optical fractionator method [ 43].

Our results may differ from those of Brown and Horn because of differences in recording method: In the current study, we used tetrodes to identify the responses of single neurons whereas the earlier results were obtained using multi-unit recordings of the activity of clusters of neurons.

Baseline images of the fluorescent retinal neurons in 30 Thy1-CFP mice were obtained using a modified confocal scanning laser ophthalmoscope.

Similar results were obtained using primary neuron cultures expressing MTS-KD-c-Src, Y193F-NDUFV2 and Y215F-SDHA.

This is approximately five times the conductance that can be calculated from published data (36 μS/cm; Koyama & Appel, 2006), which were obtained using dissociated DA neurons.